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  2. Polyclonal

GTX104589

CSB antibody [N2C1], Internal

Cannot supply to this region.

SKU:
GTX104589
Additional Names:
ERCC excision repair 6, chromatin remodeling factor , ARMD5 , CKN2 , COFS , COFS1 , CSB , CSB-PGBD3 , POF11 , RAD26 , UVSS1
Application:
IHC-P, IF, ICC
Concentration:
1.53 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Buffer:
PBS, 20% Glycerol, 0.025% ProClin 300.
Immunogen:
Recombinant protein encompassing a sequence within the center region of human CSB. The exact sequence is proprietary.
Clone:
N2C1
Uniprot:
P0DP91, Q03468
Synonyms:
ARMD5;ATP-dependent helicase ERCC6;Chimeric CSB-PGBD3 protein;Chimeric ERCC6-PGBD3 protein;CKN2;Cockayne syndrome group B protein;cockayne syndrome protein CSB;COFS;COFS1;CSB;CSB-PGBD3;DNA excision repair protein ERCC-6;ERCC6-PGBD3 fusion protein;excision repair cross-complementation group 6;excision repair cross-complementing rodent repair deficiency, complementation group 6;POF11;RAD26;UVSS1
Extra Details:
This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The protein has ATP-stimulated ATPase activity; there are contradictory publications reporting presence or absence of helicase activity. The protein appears to interact with several transcription and excision repair proteins, and may promote complex formation at repair sites. Mutations in this gene result in Cockayne syndrome type B. [provided by RefSeq]
Shipping Conditions:
Blue Ice